Data / Medical devices / Mauritius
Medical device makers in Mauritius: 4 FDA-registered establishments
4 establishments in Mauritius are registered with the FDA to make medical devices for the US market, listing 32 device types. 2 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- MauritiusCountry
Device types made here
Device types with the most registered makers in this country.
| Device | Product code | Makers |
|---|---|---|
| Needle, Hypodermic, Single Lumen | FMI | 1 |
| Set, Administration, Intravascular | FPA | 1 |
| Catheter, Continuous Flush | KRA | 1 |
| Catheter, Percutaneous | DQY | 1 |
| Implant, Orbital, Extra-Ocular | HQX | 1 |
| Knife, Ophthalmic | HNN | 1 |
| Plug, Punctum | LZU | 1 |
| Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) | HOY | 1 |
| Dilator, Lachrymal | HNW | 1 |
| Probe, Lachrymal | HNL | 1 |
| Forceps, Ophthalmic | HNR | 1 |
| Hook, Ophthalmic | HNQ | 1 |
| Specula, Ophthalmic | HNC | 1 |
| Introducer, Sphere | HNP | 1 |
| Cannula, Ophthalmic | HMX | 1 |
| Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass | DTL | 1 |
| Catheter, Angioplasty, Peripheral, Transluminal | LIT | 1 |
| Syringe, Balloon Inflation | MAV | 1 |
| Sunglasses (Non-Prescription Including Photosensitive) | HQY | 1 |
| Gauge, Measuring | JYJ | 1 |
| Catheters, Transluminal Coronary Angioplasty, Percutaneous | LOX | 1 |
| Spectacle, Magnifying | HOI | 1 |
| Frame, Spectacle | HQZ | 1 |
| Lens, Contact, Polymethylmethacrylate, Diagnostic | HJK | 1 |
| Conformer, Ophthalmic | HQN | 1 |
| Implant, Eye Sphere | HPZ | 1 |
| Lacrimal Stents And Intubation Sets | OKS | 1 |
| Cannula, Trocar, Ophthalmic | NGY | 1 |
| Crutch, Ptosis | HJZ | 1 |
| Weights, Eyelid, Implantable | NCB | 1 |
| Ocular Peg | MQU | 1 |
| Weights, Eyelid, External | MML | 1 |
Makers in Mauritius
Best documented first: most 510(k) clearances and PMA approvals.
| Maker | Location | Device types | 510(k) clearances | PMA approvals | Recall events | Source |
|---|---|---|---|---|---|---|
| Fci Sud | MAPOU LECLEZIO GOODLANDS Riviere du Rempart, Mauritius | 29 | 31 | 0 | 0 | api.fda.gov |
| Natec Medical Ltd | Moka, Mauritius | 4 | 12 | 0 | 0 | api.fda.gov |
| LILMO Ltd | Pamplemousses, Mauritius | 4 | 0 | 0 | 0 | api.fda.gov |
| Plastinax Austral Ltd | SAINT PIERRE Moka, Mauritius | 3 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.